| Tag | Content |
|---|
EnhancerAtlas ID | HS101-35600 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:131593610-131598300 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr5:131596636-131596647 | CTGAGTCATCC | - | 6.32 | | JUN(var.2) | MA0489.1 | chr5:131594268-131594282 | AGGAGGTGACTCAG | + | 6.25 | | JUNB | MA0490.1 | chr5:131596636-131596647 | CTGAGTCATCC | - | 6.14 | | NFIA | MA0670.1 | chr5:131596893-131596903 | GGTGCCAAGT | + | 6.02 | | Nfe2l2 | MA0150.2 | chr5:131596634-131596649 | GGCTGAGTCATCCTG | - | 6.17 |
|
| | Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
| SE_02077 | chr5:131592500-131597652 | Aorta | | SE_02077 | chr5:131597666-131604839 | Aorta | | SE_02422 | chr5:131592771-131597497 | Astrocytes | | SE_26291 | chr5:131593104-131604090 | Duodenum_Smooth_Muscle | | SE_27431 | chr5:131592552-131598692 | Esophagus | | SE_27887 | chr5:131593326-131596181 | Fetal_Intestine | | SE_28847 | chr5:131592746-131596199 | Fetal_Intestine_Large | | SE_36389 | chr5:131593100-131603174 | HMEC | | SE_37784 | chr5:131592672-131597826 | HSMMtube | | SE_38601 | chr5:131592507-131597671 | HUVEC | | SE_44538 | chr5:131592711-131597431 | NHDF-Ad | | SE_44873 | chr5:131592727-131597489 | NHLF | | SE_45903 | chr5:131592535-131605986 | Osteoblasts | | SE_54838 | chr5:131592088-131604374 | Stomach_Smooth_Muscle | | SE_56060 | chr5:131593504-131597890 | u87 | | SE_65894 | chr5:131592398-131597774 | Pancreatic_islets | | SE_67969 | chr5:131593504-131597890 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr5 | 131595640 | 131597275 | | chr5 | 131595834 | 131595951 | | chr5 | 131594800 | 131595180 | | chr5 | 131596993 | 131597102 | | chr5 | 131594769 | 131595694 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I132262 | chr5 | 131598280 | 131605684 |
|
Enhancer Sequence | CGAGGCTTGA AGGCGGAGGG TTGGCCTGGG CGCCCCGCAT GCTGTAGAGG CGGCTTCCAG 60
GCAGAGGCAG GCAGCCCCAG CCGCCCTCCT CCCACGCTGG GCCTGTCTGC CCGATCCCGC 120
GAAGAATCTC CCAAGAGTTC ACGCACCCGC CTCCCCGCTG GCCTCATCTG GGGGAGCCAC 180
TGTGGACCCG GGAAGGACCC GCGGAGATGG GCCAGGGGTC TAGACAGCTC TACAGAGGCC 240
CAGAAACTCT TCAGACTCAC CCCCTGCCTG AAGATCTGGG GCAAAATGAT TTAGAGCCCC 300
CCTTCCCCTA TCAGGGGTCC CTGCCGGCAG AGCTTGGTGA CCCAGGGAGG TCTGGGGTCC 360
TCGCTGAATC TGAGAAGACA GAGGTCCATC CACTTCCCAC TTTGGGCGTG AGTCAGTCTC 420
TCATTCACGA CCTCAGTCAC CCTAAGGGGA AGTGACCAGG AGGAATTTTG GCTTCCAGGG 480
GAAAGGGAGA CTTAACTGTG AGGTTGTGAG ACCCCTCCCC ACAAGATGAC ACAAAGCCGG 540
GGGCCAGGAC AGCCTCAGGC CCGTTCCTCA AGTTTCCCAG GGCCCTGCCT TGCCCACAGA 600
GAAGGAAAAG GAGCCGGCAC AGCCCTGGAG CGTGGCTAGT CTGAGGATAG AGGAGTGGAG 660
GAGGTGACTC AGGCCCTGTT CTAGGGGGTG CCTGTCTAGG GGAGACAGGA TCCTGGCCCA 720
GCCTCGACAT CCTCGTGTCT GGAGGGCCAA AAGAGAGGAC TCAGACCCTG CCCTTGGGGG 780
TCCCCAGCCT AAGGGACAGA AGAGGAGAGA ACCCAGGCCC TGCCCTTGGC GGCTCTCAGT 840
CTGGAAGGAG CAGAGGAGAT AACCTGAAAC CATCTGACGG CCATCCCTTG CTCCCACACA 900
GGCTGATCTT GTCTTTGGGG GCCTGTGTCA GAGGCACAGA GAAGCACCTT CCCCCACCCT 960
ACTGCCACCT CTTGCCATGG GGGCTGGGCC AAGCCGGCTG GGCTTTAAGA GACTTCTGTC 1020
CAGTTCTTGG GAGGGGGTGG GCACCAGGTG GAGCGTGGAA TCATGGAATC CCGTTTCTGG 1080
GGGCCAGGGT GACAGGCAGG CCCAGCTGTC CTAGGAGGCT TCCCACATCT GCCCTCACTG 1140
CCAGGTCCCT GGGGCCGAGT GAGGTGGGCC TTCAACACAT CCCAGAGCCT TTCATCTCCT 1200
CTTTCCTATA GGATTCCTGC TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TACGCAAGCC 1260
TGTGTCTGCT TGTGTGTGTC ATGCTGTGTG TCCGCTGAGG GGGCTGGTGG GGACACTAAG 1320
CGGGCTGGCC AGGCACCCTG GGCGTGAGGC CGCTGACAGG CTCAGTGGCG GCGGCTGACG 1380
GCTGCAGGCG GCAGGGAGCT GAGACATCTG TTGCCCACGC GGCTGCCTGC CCTCCGAGGA 1440
AAGGCCTCCA CACGTCACAG CTGCGGCTGC GGCAGCAGCA GCAGCAACAG CCTTGTTTGG 1500
AGCTGACTGG GGATGCAGGC CCCAGGCAGG CAGTCTGGGA GAAGGTTTGC CAGGAAGAGC 1560
CTCCTTTGTC CCCCAAAGTC ACGCGGCAGC AGCTCAGGCC CAAGGAGCCA GGATGGCTGA 1620
GGTTGGGTTT GGGTGGGATC TGGGGAGATT TACAGCGCTG GGGAGGCACA GGCCACAGCT 1680
TGCCTAGCAG GTACCTCTGG GGCAGGTCTA CAGGGACTGA AGATATGTGG GAGTGTCTTC 1740
ACCAGTGGGG CTCAAGATCC AGCCCCTCCC TTGCTTCCAG GACCTCCCCT ACGCGGGACC 1800
TGGTAGGGAG GGACAGCCTC ACACAGACAG GGAGGAGGCT ATCGGCCCGG CAGGGCTGGG 1860
GGCTTGCAAT CTCAGCCCAT GAAGCCTCCA GGAGTCCCAA GAACATCATC CGGGGCTCCT 1920
TCCCCACAAG CTATAATGAT GGCTGGCCTT GGCCAAGCAT CCAGGGTGTG CCAGGCCCTA 1980
CCCTAATGGG TGTTGGTAAC AGCTCCCTCC AGTCCCTGTA GTGAGCACCA CCTTATTTAT 2040
GCCCAGCCTC CTGTGGGGGC TTTACATGCC CTGTTTTTCT CAAATAGTCC TTACAACAGC 2100
CTTTAGAAGT AAGGACTCCC TCTGGCCTTA CATAGATGGA GACCCAGGCA CAGAGAGGCT 2160
AATGTAATCA ACCTAGAGAA GCAGAGTGGA GACAGGAGGA ATCCAGGCAG TCTGCAGTTT 2220
GCTGTGACTG TGTAGGACAA TGTGGCACCT GGTTCTGACT TGGACTCCCA GCCCACCACA 2280
TCTAGGCTGG GTGGAGCAGG GGCTGGGAAT GCAGCCACTA CCGGTAAGGG GCTGATTCAT 2340
GCCCTCACCG CCCACCTGAC TTCACTGTTC CTGTCTCTGT TCCTTCTTTC TGTTTATCCT 2400
GTGCTTAGGA GCTAGACGGA TCGGCCTGAA TTCCACTCTG TCCTGTGACT TCCCGCTTAG 2460
AGCCCTCCAT GGTTCCCAGC CACCCAGGAG AAATGCCAGC TTCCCACCCG GGTGTACAAG 2520
ACTCTGCAAT ATCTGATCCC TGCCTCTTCT CTGACTTCAT CTCTCCCACT CTCCCCTCAC 2580
TCATGATGCT CCGGCCATAC AACCTTCCTT CTTCTTTCTC TCCAGATATG CCATTATACA 2640
TGCTGGTCCT TCTGCCTGGA ACACTATCTC TCCCTCAGAT ACTCTCTTTT CCCTTACCCC 2700
CTTTGGAAGA AAAATGCAGG TGTTAAGAGC ATAGTTTTAA ATTTGGAATC AGGTGGCCTG 2760
GATTGAAATC TTGATTCAGT CTTTTATCAA TTAACTATCC TTCTGTACTT CTCTGGACCT 2820
CCGTTTCCTG ATCTAGGAAA TGGGCTTGCC TTCAGGATTA ATGAGATAAT GCATGTAAAG 2880
GTGACTGGGA GAGTCACAAT TTCTTGGCCT CACGCCCTCT CTGACCAGAA CTCCCCTAGC 2940
TCAATAGAGC TGGCAGCATC CCAGCCACCA CTGCTTTCAA GAAACTTCCT CCGCCCACAG 3000
AAGCCTGAAT GTACCCCTTG TGCTGGCTGA GTCATCCTGC CGCAGTTAGC CGCCCCCTGA 3060
AGAAAGACTC CTCTCCAGTG TGGGGACTGG GGCATGGCAT CCCTCCCCCA AGCTTCTTTC 3120
TCTTCATCTG TAAAATAGGG ATGAGAACAG CCTCTGCCTC ACCAGGTGGT TGAGGGGTTG 3180
CTGTGAGCTA GTTATGGGTA AAGCATAGAG CCCAGGCCCT GGCACAAGGC AGGTATCCAT 3240
GAAGGGGAGG AGGCAGAGGA TGGCCTTGAG GGGAGGGTGG GATGGTGCCA AGTGGGTGTC 3300
TCCCCCAGGA TGACAGGCTT GCACAGGTGC CCAGGCCCTA CAAGTGAACA TTAATGATGG 3360
GCTAGTTGGC TGAGGGTGTC ATGCTTCAGA AGAACGTTTC CTTGAGGCAG CCTACTTCAG 3420
GGCAGGTCAG CTTGGGCAGT GCCAACACCA GGCCTCCAGC CAAGGAGCTG CCAGCACCTC 3480
AGCTTTGTCC ACTCACTACT GAGACCTGGC TGAACTGAGC CTAGCTGGGC TTCCAGGAGT 3540
TCCCACCAGT AGGAGCTCCC ACCCAAAAGA ATGGGGTCAC TGGCAGCTTT TGAACCAGCT 3600
GGGCACTGGC TGGAGAGGCT GGGTAAGAAA TATATTTCTA AAGGCTATGT TGGGGTCAAG 3660
GCAGGGTGAG GGGTGCTCCA TGGCCTGGAT TCCCCTGAGT TGCTTACTTA GATATCTCTG 3720
TGAGTCTAAC TCCACCCCCC ATTCTAGCCT TCTTCAGTTG ACCAGCATTG TAAGAGCTTC 3780
CAGGTGTGAA CACTGCTTGA CCCCGAGGGG TCAATAGTGG CACTGAGGTA GCCTGAGTTC 3840
CTGTCCTGCA GGGGAAGTAG AGGTAGAATT CTGACCCCCA AACGCAGGCT GTCAGCTGGA 3900
ACTGGATGGC CCTGGACTTG CTCAGGGAGG TGATGTTCAG ACCTTCCCAT TTTAATTATA 3960
ATGAAGTATT AACATGAACA GTGTAGGGGG AAAAGGTGGT CATGGGAGCA CACTGGGTAG 4020
TGAGATCCCA GAGAGGCTCC CAGAGGAAGT GGCCTCTATG CTGAGATCTG AAGGATGAGG 4080
ATGTGGGAGT CAAAGGAATG TTCCAGGTGG AGGGAGCAGC TTTTGCAGAA GTGTAGAGGT 4140
GAGTGATATA TGGTGCCTGT GAGCACCCCA TAGACATTCA CATGGTCTGG ACAGAGTGTG 4200
GGTGTGGAGG TGGGGATGAG AGTTGAAATC AAGCAAGTAG GAAGGCAAGG TCACTAAGGG 4260
TTTGAATATT AGGTCAAGGT GTGTAGTCTG TCTGGTTGGG GCCTTGTCTG TGTAGGGTAT 4320
CTGTGATATG TCCATGCTGT GTATGTATCT GTGAGCACCT ATGTCTCCAT GTGTCTCTGT 4380
GTCCCCTGCA TGTCCTTGGG CACATACGCA GGCTGCAAGA ACAACATCCA TTTGTCCCAG 4440
CCCTGAGGAA GCCCTTCTCG TATATCCTCA TGCCCTGCCA GGCCTCCAGG TGCTGGAGTT 4500
GGAGGTGTTT CCAGCAAGGC TGCAGCCAGG CTACATGGGG ACCTCAACCA GCCACTCGGC 4560
TTGCCCATCC ACAGGCCATG CTGGTAGCAG GCCACACTGG CTAGGTTCTG AGGTTGGAGG 4620
AGGCCTAGGG CACAGCTTGC AGCAAGACCA TATCATGACT GTGCCCAGCC ATCTGGCTTG 4680
TCTGCTCGCA 4690
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